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Rorbhstp
Spontaneous Allele Detail
Summary
Symbol: Rorbhstp
Name: RAR-related orphan receptor beta; high stepper
MGI ID: MGI:3846436
Synonyms: h1
Gene: Rorb  Location: Chr19:18907969-19088560 bp, - strand  Genetic Position: Chr19, 13.28 cM
Alliance: Rorbhstp page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Spontaneous
Mutation:    Duplication
 
Mutation detailsThis spontaneous mutation is an approximately 326 kb duplication from Chromosome 19 19,010,565 bp to 19,336,747 bp (GRCm38), which includes the first exon of this gene. Transcript levels in the brain are decreased but not in the retina. Abnormal transcripts were not found by 5-prime RACE. (J:222308, J:337403)
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(s)
In Structures Affected by this Mutation: 1 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Rorb Mutation:  38 strains or lines available
References
Original:  J:148753 Harris B, et al., High Stepper: A new neurological and eye mutation is mapped to Chromosome 19. MGI Direct Data Submission. 2009;
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory